DisGeNET is a knowledge management platform that integrates and standardizes the data of genes and mutations related to diseases from multiple sources. It covers entire range of human disease.
Source | Last Updated |
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DisGeNET | July 29, 2024 |
Disease ID | Disease Name ▲ | Gene Symbol | Gene ID | Gene Name | UniProt ID |
---|---|---|---|---|---|
C0036857 | Severe intellectual disability | POMT1 | 10585 | protein O-mannosyltransferase 1 | Q9Y6A1 |
C0036857 | Severe intellectual disability | DPAGT1 | 1798 | dolichyl-phosphate N-acetylglucosaminephosphotransferase 1 | Q9H3H5 |
C0036857 | Severe intellectual disability | ALG14 | 199857 | ALG14 UDP-N-acetylglucosaminyltransferase subunit | Q96F25 |
C0036857 | Severe intellectual disability | FKTN | 2218 | fukutin | O75072 |
C0036857 | Severe intellectual disability | SLC35A3 | 23443 | solute carrier family 35 member A3 | Q9Y2D2 |
C0036857 | Severe intellectual disability | POMT2 | 29954 | protein O-mannosyltransferase 2 | Q9UKY4 |
C0036857 | Severe intellectual disability | PIGW | 284098 | phosphatidylinositol glycan anchor biosynthesis class W | Q7Z7B1 |
C0036857 | Severe intellectual disability | PIGC | 5279 | phosphatidylinositol glycan anchor biosynthesis class C | Q92535 |
C0036857 | Severe intellectual disability | MGAT2 | 4247 | alpha-1,6-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase | Q10469 |
C0036857 | Severe intellectual disability | POMGNT1 | 55624 | protein O-linked mannose N-acetylglucosaminyltransferase 1 (beta 1,2-) | Q8WZA1 |
C0036857 | Severe intellectual disability | PIGV | 55650 | phosphatidylinositol glycan anchor biosynthesis class V | Q9NUD9 |
C0036857 | Severe intellectual disability | ST3GAL3 | 6487 | ST3 beta-galactoside alpha-2,3-sialyltransferase 3 | Q11203 |
C0036857 | Severe intellectual disability | ALG13 | 79868 | ALG13 UDP-N-acetylglucosaminyltransferase subunit | Q9NP73 |
C0036857 | Severe intellectual disability | ST3GAL5 | 8869 | ST3 beta-galactoside alpha-2,3-sialyltransferase 5 | Q9UNP4 |
C0036857 | Severe intellectual disability | LARGE1 | 9215 | LARGE xylosyl- and glucuronyltransferase 1 | O95461 |
C0036857 | Severe intellectual disability | PIGO | 84720 | phosphatidylinositol glycan anchor biosynthesis class O | Q8TEQ8 |
C0036857 | Severe intellectual disability | FKRP | 79147 | fukutin related protein | Q9H9S5 |
C0036857 | Severe intellectual disability | MAN1B1 | 11253 | mannosidase alpha class 1B member 1 | Q9UKM7 |
C0036857 | Severe intellectual disability | COG5 | 10466 | component of oligomeric golgi complex 5 | Q9UP83 |
C0036857 | Severe intellectual disability | FUCA1 | 2517 | alpha-L-fucosidase 1 | P04066 |
C0036857 | Severe intellectual disability | NAGA | 4668 | alpha-N-acetylgalactosaminidase | P17050 |
C0036857 | Severe intellectual disability | NAGLU | 4669 | N-acetyl-alpha-glucosaminidase | P54802 |
C0036857 | Severe intellectual disability | TUSC3 | 7991 | tumor suppressor candidate 3 | Q13454 |
C0036857 | Severe intellectual disability | SRD5A3 | 79644 | steroid 5 alpha-reductase 3 | Q9H8P0 |
C0036857 | Severe intellectual disability | RFT1 | 91869 | RFT1 homolog | Q96AA3 |
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Last updated: August 19, 2024